chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1232068986232068987GA16GENICpossibly homozygous62103388
1232070375232070376CA9GENICpossibly homozygous62103389
1232070514232070515TC22GENICpossibly homozygous62103390
1232071112232071115TTG---9GENIChomozygous62103391
1232074964232074965CT6GENIChomozygous62103392
1232076367232076368AG18GENIChomozygous62103393
1232077014232077015AG25GENIChomozygous61119000
1232078063232078064CT16GENIChomozygous62103394